Disease Directory Familial hypofibrinogenemia
Rare Disease

Familial hypofibrinogenemia

Type

Clinical subtype

Gene

FGA, FGB, FGG

About Familial hypofibrinogenemia

Familial hypofibrinogenemia is a rare disease catalogued by Orphanet (ORPHA:101041). It is associated with the FGA, FGB, FGG genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Familial hypofibrinogenemia trials.

Search ClinicalTrials.gov for "Familial hypofibrinogenemia" or filter by Orphanet code ORPHA:101041 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:101041)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Familial hypofibrinogenemia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial hypofibrinogenemia. Updated daily.